Summary of Key Points WHO Position Paper on BCG Vaccine, February 2018 1
Introduction This position paper replaces the 2004 WHO position paper on Bacille Calmette-Guérin (BCG) vaccine and the 2007 WHO revised BCG vaccination guidelines for infants at risk for human immunodeficiency virus (HIV) infection. It incorporates recent developments in the field of tuberculosis (TB), provides guidance on the immunization of children infected with HIV, re-emphasizes the importance of the BCG birth dose and outlines the urgent need for research in the development of new vaccines This position paper also includes recommendations for the prevention of leprosy. 2
Background Tuberculosis (TB) is caused by the bacterium Mycobacterium tuberculosis, which spreads via airborne droplets when individuals infected with active TB cough. HIV infection, malnutrition, tobacco use, and diabetes are predisposing factors for TB. Multi-drug resistant TB (MDR-TB) is caused when bacteria do not respond to the 2 most powerful first line anti-tb drugs. Globally, 1.7 billion people are estimated to be infected with M. tuberculosis and in 2016, 1.7 million people died from TB, including 400,000 among people infected with HIV. In children, TB most commonly occurs in those aged <5 years. 3
Background Leprosy is caused by Mycobacterium leprae and mainly affects the skin and peripheral nerves. More than 200,000 cases of Leprosy were reported in 2016, including 12,819 new cases with visible deformities. Buruli ulcer is caused by Mycobacterium ulcerans and In 2016, 1,864 new cases of Buruli ulcer were reported from 11 countries. 4
Vaccines Bacillus Calmette-Guérin (BCG) vaccines continue to be the only vaccines in use for prevention of TB. BCG is a live attenuated bacterial vaccine derived from M. bovis. Several BCG vaccines, based on different strains, are available worldwide. BCG has demonstrated significant effectiveness, however protection has not been consistent across all forms in all age groups BCG has also shown effectiveness in preventing leprosy (RR from 20-80%), Buruli ulcer (RR of 50% in Africa region) and other non-tuberculosis mycobacterial (NTM) infections. Several new vaccine candidates are in development to protect against TB and Leprosy. 5
Vaccine Safety About 95% of BCG vaccine recipients experience a reaction at the injection site that heals within 2-5 months leaving a superficial scar, this is considered normal. Adverse events following (AEFI) are dependent on the strain used, number of viable bacilli in the batch and variation in injection technique. Disseminated BCG disease may occur between 1.56 and 4.29 cases per million doses and can have an incidence of up to 1% of infants and HIV-infected children. 6
Vaccine Effectiveness A systematic review of 12 cohort studies found protection against Pulmonary TB (PTB) ranged from 44-99% in 11 studies and no protection in one study. Protection varies by age: Neonatal vaccination provided 82% protection against TB (RR 0.18, 95% CI: 0.15 0.21). In school-age TST-negative children BCG was 64% protective against PTB (RR 0.36, 95% CI: 0.30 0.42). A systematic review of 5 studies found BCG was effective in preventing leprosy (RR 0.45 CI: 0.34 0.56) however there was considerable heterogeneity (I 2 =98%) 7
WHO Position BCG vaccination is recommended in countries or settings with a high incidence of TB and/or high leprosy burden as well as where Buruli ulcer occurs. A single dose should be given to all healthy neonates at birth. If the vaccine cannot be administered at birth, it should be given at the earliest opportunity thereafter. Countries with low incidence of TB or leprosy may choose to selectively vaccinate high-risk neonates. Countries with declining rates of TB are encouraged to evaluate the epidemiology of TB and leprosy and consider a switch to selective risk group vaccination. 8
WHO Position Standard dose of BCG vaccine is an intradermal injection of 0.05 ml of the reconstituted vaccine for infants <1 year, and 0.1 ml for those >1 year. BCG multi-dose vials should be used despite any wastage. BCG vaccine can be safely co-administered with other routine childhood vaccines including the hepatitis B birth dose. Revaccination is not recommended even if the tuberculin skin testing (TST) reaction or result of an IFN-ɣ release assay (IGRA) is negative. 9
Special Populations WHO Position BCG is recommended for unvaccinated, TST-negative or IGRA-negative school children for those coming from or moving to high incidence/burden settings, as well as older groups at risk through occupational exposure. As a precaution, BCG vaccination is not recommended during pregnancy. BCG vaccination is contraindicated for immunocompromised persons and for patients undergoing immunosuppressive treatment. 10
WHO Position Children who are HIV-infected should not receive BCG vaccination. HIV-infected individuals, including children, who are receiving anti-retroviral therapy (ART), are clinically well and immunologically stable should be vaccinated. Neonates born to women of unknown HIV status should be vaccinated. 11
WHO Position Neonates with unknown HIV status born to HIV-infected women should be vaccinated if they have no clinical evidence suggestive of HIV infection, regardless of whether the mother is receiving ART Neonates with HIV infection should delay BCG vaccination until ART has been started and are immunologically stable. Neonates born to mothers with pulmonary TB should receive BCG vaccination if they are asymptomatic, have no immunological evidence of TB and are HIV-negative 12
Future Research Needs Further reporting of TB cases is needed to better understand the safety and effectiveness of BCG vaccination at different ages and in different populations, especially of HIV-infected children including those receiving ART. Further evidence of programmatic strategies such as timeliness and wastage is needed. Development of additional vaccines that provide greater protection for all ages and populations. More effective vaccines against leprosy is needed 13
For more information on the WHO BCG position paper, please visit the WHO website: www.who.int/immunization/documents/positionpapers